Trials / Completed
CompletedNCT06955871
Clinical Investigation of Bleeding Reduction Efficacy on Toothpaste Containing 1.05% Chitosan
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 134 (actual)
- Sponsor
- Colgate Palmolive · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the bleeding reduction efficacy of toothpaste containing 1.05% Chitosan compared to a regular fluoride toothpaste, and compared to a toothpaste containing 67% bicarbonate.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Toothpaste containing 1.05% Chitosan | Toothpaste containing 1.05% Chitosan |
| OTHER | Silica-based NaF Toothpaste | Silica-based NaF Toothpaste |
| OTHER | Toothpaste with 67% bicarbonate | Toothpaste containing 67% Bicarbonate |
Timeline
- Start date
- 2025-04-29
- Primary completion
- 2025-06-04
- Completion
- 2025-06-04
- First posted
- 2025-05-02
- Last updated
- 2025-08-15
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06955871. Inclusion in this directory is not an endorsement.